Luwi, LLC is one of 14005 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Luwi, LLC - FDA 510(k) Cleared Devices
Recent clearances: LIXI (LXOSFM1)
1
Total
1
Cleared
0
Denied
Luwi, LLC has 1 FDA 510(k) cleared medical devices. Based in Mount Prospect, US.
Latest FDA clearance: Jul 2026. Active since 2026. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Luwi, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Rook Quality Systems as regulatory consultant.
FDA 510(k) Regulatory Record - Luwi, LLC
1 devices